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番茄黄化曲叶病毒与番茄奇诺拉巴斯病毒共同侵染墨西哥南下加利福尼亚州辣椒的首次报道

First Report of Tomato yellow leaf curl virus Co-infecting Pepper with Tomato chino La Paz virus in Baja California Sur, Mexico.

作者信息

Cardenas-Conejo Y, Arguello-Astorga G, Poghosyan A, Hernandez-Gonzalez J, Lebsky V, Holguin-Peña J, Medina-Hernandez D, Vega-Peña S

机构信息

Instituto Potosino de Investigación Cientifica y Tecnologica (IPICYT), San Luis Potosí, 78216, Mexico.

Centro de Investigaciones Biológicas del Noroeste (CIBNOR), La Paz, BCS, 23090, Mexico.

出版信息

Plant Dis. 2010 Oct;94(10):1266. doi: 10.1094/PDIS-06-10-0444.

Abstract

Chile peppers are among the most common and important crops in the State of Baja California Sur, Mexico, where diverse varieties of this crop are annually cultivated. The "chile ancho" (Capsicum annuum L. var. ancho poblano) is one of the most popular hot peppers that is exported fresh to the United States. During a survey in December of 2007 in an experimental field of the CIBNOR in El Carrizal, one of the principal farm districts in the state, a high incidence of yellowing, stunted growth with shortened internodes, foliage discoloration, malformation and crinkle, abortion of flowers, and reduction in size and quantity of fruit were noted in chile ancho. Symptoms and the presence of large populations of whiteflies in the field suggested a possible viral etiology of disease. The symptoms of disease were successfully transmitted by grafting from field plants to tomato and pepper test plants. Samples from both field and test plants were analyzed by scanning electron microscopy (SEM) and molecular techniques. SEM study revealed groups of geminate particles characteristic of begomoviruses (Geminiviridae) in phloem tissue of randomly selected symptomatic plants (four field and two test plants). Total DNA from 12 symptomatic plants (eight naturally infected and four test plants) was obtained by a modified Dellaporta method and analyzed by PCR using the begomovirus universal primers prRepDGR (2) and prC889 (3). Amplicons of ~1.4 kb were obtained from all plant samples and PCR products from four of them were cloned into pGEM-T Easy vector (Promega, Madison, WI) and subsequently analyzed by restriction fragment length polymorphism (RFLP) using EcoRI and HinfI. Two distinct restriction fragment patterns were observed among the cloned PCR products, indicating the occurrence of at least two viruses in the infected plant tissues. The four examined samples contained the same two begomoviruses according to the RFLP analysis data. The complete sequence of the genomic component A of those viruses was determined by PCR amplification of viral DNA with universal, degenerate primers previously described (2), the subsequent cloning of overlapped PCR products, and sequencing. The full-length DNA-A sequence was assembled and compared with viral sequences available at the GenBank database using BlastN and the ClustalV alignment method (MegAlign; DNASTAR, Madison, WI). The 2,781-bp complete genome sequence of one co-infecting monopartite begomovirus (Accession No. HM459851) displayed the highest identity (99%) with Tomato yellow leaf curl virus (TYLCV), isolate Guasave, Sinaloa (Accession No. FJ609655). The 2,609-bp DNA-A sequence of the second begomovirus exhibited the highest nucleotide identity (96%) with Tomato chino La Paz virus (ToChLPV)-[Baja California Sur] (Accession No. AY339619). The presence of TYLCV in this region of Mexico had not been previously reported nor was ToChLPV detected in pepper until now. To our knowledge, this is the first report of a mixed infection of pepper plants with TYLCV and a bipartite begomovirus in Baja California Peninsula. Since the high frequency of recombination events observed in begomovirus mixed infections involving TYLCV (1), it would be important to monitor the possible emergence of ToChLPV-TYLCV recombinants with higher potential virulence. References: (1) S. García-Andrés et al. Virology 365:210, 2007. (2) A. Mauricio-Castillo et al. Plant Dis. 91:1513, 2007. (3) S. D. Wyatt and J. K. Brown. Phytopathology 86:1288, 1996.

摘要

辣椒是墨西哥南下加利福尼亚州最常见且重要的作物之一,该州每年种植多种辣椒品种。“ancho辣椒”(辣椒属辣椒种var. ancho poblano)是最受欢迎的辣椒品种之一,以新鲜的形式出口到美国。2007年12月,在该州主要农业区之一卡里萨尔的CIBNOR试验田进行的一项调查中,发现ancho辣椒出现了高发病率的黄化、节间缩短导致的生长发育不良、叶片变色、畸形和皱缩、花朵败育以及果实大小和数量减少等情况。田间出现的症状以及大量粉虱表明该病可能由病毒引起。通过将田间植株嫁接到番茄和辣椒试验植株上,成功传播了该病症状。对田间植株和试验植株的样本进行了扫描电子显微镜(SEM)分析和分子技术分析。SEM研究在随机选择的有症状植株(4株田间植株和2株试验植株)的韧皮部组织中发现了双生病毒科双生病毒特征性的双生粒子群。采用改良的Dellaporta方法从12株有症状植株(8株自然感染植株和4株试验植株)中提取总DNA,并使用双生病毒通用引物prRepDGR(2)和prC889(3)进行PCR分析。所有植株样本均获得了约1.4 kb的扩增子,其中4个样本的PCR产物被克隆到pGEM-T Easy载体(Promega公司,威斯康星州麦迪逊)中,随后使用EcoRI和HinfI进行限制性片段长度多态性(RFLP)分析。在克隆的PCR产物中观察到两种不同的限制性片段模式,表明受感染的植物组织中至少存在两种病毒。根据RFLP分析数据,4个检测样本含有相同的两种双生病毒。通过使用先前描述的通用简并引物对病毒DNA进行PCR扩增、随后克隆重叠的PCR产物并测序,确定了这些病毒基因组组分A的完整序列。将全长DNA-A序列进行组装,并使用BlastN和ClustalV比对方法(MegAlign;DNASTAR公司,威斯康星州麦迪逊)与GenBank数据库中可用的病毒序列进行比较。一种共同感染的单分体双生病毒(登录号HM459851)的2781 bp完整基因组序列与番茄黄化曲叶病毒(TYLCV)瓜萨韦分离株(锡那罗亚州,登录号FJ609655)的同源性最高(99%)。第二种双生病毒的2609 bp DNA-A序列与番茄奇诺拉巴斯病毒(ToChLPV)-[南下加利福尼亚州](登录号AY339619)的核苷酸同源性最高(96%)。此前在墨西哥该地区尚未报道过TYLCV的存在,直到现在也未在辣椒中检测到ToChLPV。据我们所知,这是首次报道在南下加利福尼亚半岛辣椒植株中TYLCV和一种双分体双生病毒的混合感染。由于在涉及TYLCV的双生病毒混合感染中观察到高频率的重组事件(1),监测具有更高潜在毒力的ToChLPV-TYLCV重组体的可能出现将非常重要。参考文献:(1) S. García-Andrés等人,《病毒学》365:210,2007年。(2) A. Mauricio-Castillo等人,《植物病害》91:1513,2007年。(3) S. D. Wyatt和J. K. Brown,《植物病理学》86:1288,1996年。

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